Actively Recruiting
Segmental Vibrator With NMES on Lower Limb Function in Subacute Stroke
Led by Riphah International University · Updated on 2025-08-19
50
Participants Needed
1
Research Sites
24 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Stroke is one of the world's leading causes of death and disability. It can cause a variety of motor disorders, such as apraxia, sensory deficits, abnormal muscle tone, inadequate weight transfer, lack of fine motor skills, incoordination, and balance deficit. These disorders can have a significant negative impact on a person's quality of life.
CONDITIONS
Official Title
Segmental Vibrator With NMES on Lower Limb Function in Subacute Stroke
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Both male and female patients were included in the study.
- Age between 45 and 60 years.
- Diagnosed with ischemic stroke.
- Experienced sub-acute ischemic stroke, 15 days to 12 weeks post-stroke.
- Montreal Cognitive Assessment scores between 18 and 24.
- Modified Ashworth scale scores less than +1.
- National Institutes of Health Stroke Scale (NIHSS) scores between 1 and 15.
- No pain felt from the vibrator.
- Able to give informed consent or have a legal representative to do so.
You will not qualify if you...
- History of serious neurological or mental conditions other than stroke that affect lower limb motor recovery.
- Severe arthritis or joint injuries interfering with treatment or evaluations.
- Significant hearing or vision impairments affecting treatment or evaluations.
- Undergoing anti-spatial therapy or other clinical trials.
- Bilateral brain lesions.
- Ischemic involvement of the cerebellum or basal ganglia.
- Presence of metal implants such as cardiac pacemaker.
- Skin lesions at the site of stimulation electrodes.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Jinnah Hospital
Lahore, Punjab Province, Pakistan, 54660
Actively Recruiting
Research Team
A
Aruba Saeed, Phd
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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